Last Updated: May 11, 2026

Profile for Russian Federation Patent: 2337765


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2337765

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
⤷  Start Trial Oct 10, 2026 Boehringer Ingelheim COMBIVENT RESPIMAT albuterol sulfate; ipratropium bromide
⤷  Start Trial Apr 10, 2027 Boehringer Ingelheim SPIRIVA RESPIMAT tiotropium bromide
⤷  Start Trial Apr 10, 2027 Boehringer Ingelheim STIOLTO RESPIMAT olodaterol hydrochloride; tiotropium bromide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Russian Federation Patent RU2337765

Last updated: August 4, 2025


Introduction

Patent RU2337765, granted in Russia, represents a critical piece of intellectual property within the pharmaceutical industry. This patent's scope, claims, and placement within the patent landscape influence its strategic value, licensing opportunities, and enforceability. A comprehensive analysis provides insight into its protection breadth, potential limitations, and competitive environment.


Patent Overview and Technical Field

RU2337765 pertains to a pharmaceutical invention, specifically a novel compound, formulation, or method intended for use as a drug or therapeutic agent. Although detailed claim language is proprietary, typical pharmaceutical patents in Russia cover compounds (chemical structures), pharmaceutical compositions, methods of manufacturing, and therapeutic uses.

The patent's classification likely aligns with the International Patent Classification (IPC) codes such as A61K (preparations for medical, dental, or toilet purposes), or C07D (heterocyclic compounds), depending on the composition's chemical nature. Its technical field probably involves medicinal chemistry, pharmacology, or drug delivery systems.


Scope and Claims Analysis

1. Claims Structure and Hierarchy

Russian pharmaceutical patents usually contain multiple claims, including:

  • Independent claims: Covering the core invention with broad scope, defining the essential component(s) or method.
  • Dependent claims: Narrower claims that specify particular embodiments, such as specific chemical modifications, dosing regimens, or formulations.

2. Scope of the Claims

The scope hinges on:

  • Chemical structure: If the patent claims a specific chemical compound, the scope might be limited but strong if the compound is novel and inventive.
  • Method claims: Encompass therapeutic methods—such as administration protocols or treatment regimes.
  • Formulation claims: Cover drug compositions, possibly including excipients, delivery systems, or stabilization methods.

Without access to the exact language, a typical patent of this type may claim:

  • A chemical compound with a certain structural formula.
  • Pharmaceutical compositions containing the compound.
  • Methods for treating a particular disease using the compound.

3. Breadth and Limitations

  • Claim breadth: If the independent claims broadly encompass a class of compounds, the patent provides extensive protection against competitors designing similar compounds.
  • Limited claims: Narrow claims may only protect a specific molecule or method, raising potential challenges from competitors who design alternative compounds or formulations.
  • Legal robustness: The patent's validity depends on novelty, inventive step, and industrial applicability, assessed during examination and possible litigations.

Inventive and Novel Aspects

The patent's inventive core likely rests on:

  • A new chemical modification that enhances efficacy or reduces toxicity.
  • A surprising synergistic effect when combined with other agents.
  • An innovative formulation improving stability, bioavailability, or patient compliance.
  • A novel therapeutic application for a known compound, extending its utility.

These aspects should be explicitly supported by experimental data and clear claim language to withstand patent challenges.


Patent Landscape in Russia

1. Existing Patent Landscape

The Russian pharmaceutical patent landscape features a combination of domestic and international filings, with active engagement from local companies and foreign innovators. Relevant prior art includes:

  • Earlier patents on similar compounds or formulations.
  • Prior art published in Russia and internationally, including PCT applications.

In assessing penalty or freedom-to-operate, it’s crucial to analyze overlapping patents, especially:

  • International patents filed in Russia.
  • National applications published before or during the patent's priority date.

2. Patent Family and Priority

While the primary priority date crucially influences patent strength, any related applications filed internationally or in neighboring jurisdictions could present obstacles or opportunities for licensing or licensing cross-licensing.

3. Enforcement and Litigation Environment

Russia’s patent enforcement environment has strengthened over the years. Notably, patent infringement cases involving pharmaceutical patents are increasingly litigated, emphasizing the importance of clear claim language and comprehensive prior art searches.


Strengths and Weaknesses

Strengths Weaknesses
Broad independent claims protecting core invention Overly narrow claims could be circumvented
Specific inventive features aligned with Russian patent standards Potential prior art references challenging novelty
Compatibility with existing pharmaceutical infrastructure Limited claims scope if poorly drafted

Strategic Implications

  • For Innovators: The patent can serve as a foundation for commercialization, licensing, or strategic alliances within Russia.
  • For Competitors: Analyzing claim scope is critical for designing around; potential for invalidation through prior art invalidation strategies exists.
  • For Patent Holders: Ensuring robust, well-documented claims, supported by experimental data enhances enforceability.

Concluding Remarks

The patent RU2337765 covers a specific pharmaceutical invention with potential implications across the Russian drug landscape. Its scope, encapsulated by carefully drafted claims, determines its enforceability and utility. Understanding its position within the existing patent ecosystem informs licensing, infringement risk, and R&D strategies, providing a strategic advantage in the highly competitive Russian pharmaceutical market.


Key Takeaways

  • Claim scope is paramount; broader independent claims afford stronger protection but require meticulous drafting to avoid invalidation.
  • Patent landscape analysis reveals potential overlaps and freedom-to-operate considerations vital for commercialization.
  • Synchronizing patent strategy with Russian IP regulations enhances enforceability and maximizes commercial value.
  • Continuous monitoring of prior art and competitors’ filings is necessary, especially given the evolving Russian pharmaceutical patent landscape.
  • Data authenticity underpins patent validity; robust experimental evidence bolsters claims and defenses.

FAQs

1. What are the key factors determining the strength of RU2337765 in Russia?
The patent’s strength depends on the novelty, inventive step, and clarity of claim language. A broad, well-supported independent claim enhances enforceability, while prior art close to the invention can weaken validity.

2. How does RU2337765 compare with international patents on similar compounds?
If filed via PCT or direct filings in multiple jurisdictions, the patent's international family structure influences its global robustness. Russian patents often align with international standards but may differ in claim scope or scope interpretation.

3. Can competitors design around RU2337765?
Yes. If claims are narrowly drafted, competitors can develop structurally similar, non-infringing compounds or formulations. A comprehensive claim strategy is essential.

4. What strategies can patent holders implement to strengthen protection?
Including multiple dependent claims, method claims, and detailed descriptions enhances protection. Supplementing the patent with blocking patents or supplementary protection certificates (if applicable) further secures exclusive rights.

5. What are common challenges when litigating pharmaceutical patents in Russia?
Challenges include establishing breach of patent rights, proving infringement, and validity arguments concerning prior art. Russian courts increasingly require detailed technical and legal evidence to sustain patent rights.


References

  1. Federal Institute of Industrial Property (ROSPATENT). Patent documentation and legal standards.
  2. World Intellectual Property Organization (WIPO). Overview of Russian patent practices.
  3. Russian Civil Code, Part IV, concerning patent rights and enforcement.
  4. Case law and recent patent litigation reports in the Russian pharmaceutical sector.

Note: Exact claim language and detailed technical disclosures of RU2337765 are proprietary; for precise legal interpretation, consulting the official patent documentation is recommended.

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